Evidence map›Paper›PMID 35585045›Full record

ArticleNature communications2022

HDLBP binds ER-targeted mRNAs by multivalent interactions to promote protein synthesis of transmembrane and secreted proteins.

Ulrike Zinnall, Miha Milek, Igor Minia, Carlos H Vieira-Vieira, Simon Müller, Guido Mastrobuoni, Orsalia-Georgia Hazapis, Simone Del Giudice, David Schwefel, Nadine Bley and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Disrupted diencephalon development and neuropeptidergic pathways in zebrafish with autism-risk mutations.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Translation of circular RNAs.Nucleic acids research · 2025
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  18. Review
  19. Specialized Ribosomes in Health and Disease.International journal of molecular sciences · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 3 countries.

Ulrike Zinnall *Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0002-0782-7751
Miha Milek *Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany. miha.milek@bih-charite.de.ORCID 0000-0002-0803-8439
Igor MiniaMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.
Carlos H Vieira-VieiraMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0001-5443-4507
Simon MüllerInstitute of Molecular Medicine, Medical Faculty, Martin Luther University, Halle, Germany.
Guido MastrobuoniMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0003-4509-1295
Orsalia-Georgia HazapisMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.
Simone Del GiudiceMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0003-0194-3767
David SchwefelCharite-Universitätsmedizin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute of Medical Physics and Biophysics, Berlin, Germany.ORCID 0000-0002-2945-0908
Nadine BleyInstitute of Molecular Medicine, Medical Faculty, Martin Luther University, Halle, Germany.
Franka VoigtFriedrich Miescher Institute for Biomedical Research, 4058, Basel, Switzerland.
Jeffrey A ChaoFriedrich Miescher Institute for Biomedical Research, 4058, Basel, Switzerland.ORCID 0000-0002-5895-9156
Stefan KempaMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0002-0696-9299
Stefan HüttelmaierInstitute of Molecular Medicine, Medical Faculty, Martin Luther University, Halle, Germany.ORCID 0000-0001-9335-4227
Matthias SelbachMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany.ORCID 0000-0003-2454-8751
Markus LandthalerMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin Institute for Medical Systems Biology, Berlin, Germany. markus.landthaler@mdc-berlin.de.ORCID 0000-0002-1075-8734
Max Delbrück Center · DEMartin Luther University Halle-Wittenberg · DEFriedrich Miescher Institute · CHHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biological role of RNA-binding proteins in the secretory pathway is not well established. Here, we describe that human HDLBP/Vigilin directly interacts with more than 80% of ER-localized mRNAs. PAR-CLIP analysis reveals that these transcripts represent high affinity HDLBP substrates and are specifically bound in their coding sequences (CDS), in contrast to CDS/3'UTR-bound cytosolic mRNAs. HDLBP crosslinks strongly to long CU-rich motifs, which frequently reside in CDS of ER-localized mRNAs and result in high affinity multivalent interactions. In addition to HDLBP-ncRNA interactome, quantification of HDLBP-proximal proteome confirms association with components of the translational apparatus and the signal recognition particle. Absence of HDLBP results in decreased translation efficiency of HDLBP target mRNAs, impaired protein synthesis and secretion in model cell lines, as well as decreased tumor growth in a lung cancer mouse model. These results highlight a general function for HDLBP in the translation of ER-localized mRNAs and its relevance for tumor progression.

Indexed as

Membrane ProteinsRNA-Binding ProteinsRNA, Messenger3' Untranslated RegionsAnimalsCell LineCytosolEndoplasmic ReticulumHumansMiceProtein BiosynthesisSignal Recognition Particle3' Untranslated Regionshigh density lipoprotein binding proteinMembrane ProteinsRNA-Binding ProteinsRNA, MessengerSignal Recognition Particle

Identifiers

PMID35585045
PMCPMC9117268
OpenAlexW4280551763

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.